CXCR5<sup>+</sup>PD-1<sup>+</sup> follicular helper CD8 T cells control B cell tolerance.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 31562329.
- Also identified by DOI 10.1038/s41467-019-12446-5 and PMC identifier 6765049.
- Licence recorded as CC BY.
- The licence permits redistribution, so the abstract is shown in full and the full text is available from the publisher.
Abstract
Many autoimmune diseases are characterized by the production of autoantibodies. The current view is that CD4<sup>+</sup> T follicular helper (Tfh) cells are the main subset regulating autoreactive B cells. Here we report a CXCR5<sup>+</sup>PD1<sup>+</sup> Tfh subset of CD8<sup>+</sup> T cells whose development and function are negatively modulated by Stat5. These CD8<sup>+</sup> Tfh cells regulate the germinal center B cell response and control autoantibody production, as deficiency of Stat5 in CD8 T cells leads to an increase of CD8<sup>+</sup> Tfh cells, resulting in the breakdown of B cell tolerance and concomitant autoantibody production. CD8<sup>+</sup> Tfh cells share similar gene signatures with CD4<sup>+</sup> Tfh, and require CD40L/CD40 and TCR/MHCI interactions to deliver help to B cells. Our study thus highlights the diversity of follicular T cell subsets that contribute to the breakdown of B-cell tolerance.
Medical subject headings
- B-Lymphocytes
- CD8-Positive T-Lymphocytes
- Immune Tolerance
- Programmed Cell Death 1 Receptor
- Receptors, CXCR5
- T-Lymphocytes, Helper-Inducer